A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892551



Internal ID18836685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:60207981..60223913hg38UCSC Ensembl
Outerchr14:60207981..60223913hg38UCSC Ensembl
Innerchr14:60674699..60690631hg19UCSC Ensembl
Outerchr14:60674699..60690631hg19UCSC Ensembl
Innerchr14:59744452..59760384hg18UCSC Ensembl
Outerchr14:59744452..59760384hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3815933
hg1915933
hg1815933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797209
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892551
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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